NM_000891.3(KCNJ2):c.901A>C (p.Met301Leu) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 13, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000535723.7
Allele description [Variation Report for NM_000891.3(KCNJ2):c.901A>C (p.Met301Leu)]
NM_000891.3(KCNJ2):c.901A>C (p.Met301Leu)
Condition(s)
- Name:
- Andersen Tawil syndrome (LQT7)
- Synonyms:
- Andersen Syndrome; Andersen cardiodysrhythmic periodic paralysis; Long QT syndrome 7; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0008222; MedGen: C1563715; Orphanet: 37553; OMIM: 170390
-
Gloeothece sp. PCC 6909 acetyl-CoA-acetyltransferase (phaA) gene, complete cds
Gloeothece sp. PCC 6909 acetyl-CoA-acetyltransferase (phaA) gene, complete cdsgi|829624541|gb|KR231686.1|Nucleotide
-
BP686492 Osada Taira anterior neuroectoderm (ANE) pCS105 cDNA library Xenopus la...
BP686492 Osada Taira anterior neuroectoderm (ANE) pCS105 cDNA library Xenopus laevis cDNA clone XL451g14ex 5', mRNA sequencegi|46034447|gnl|dbEST|24551525|dbj| 492.1|Nucleotide
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Last Updated: Sep 29, 2024